Relevant bibliographies by topics / Cadmium selenide

Academic literature on the topic 'Cadmium selenide'

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Published: 4 June 2021
Last updated: 30 May 2022

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Journal articles on the topic "Cadmium selenide"

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Zhang, Ya Hui, Xi Cheng, and Qing Wang. "The Synthesis of Cadmium Sulfide and Cadmium Selenide Nanostructures." Applied Mechanics and Materials 423-426 (September 2013): 467–70. http://dx.doi.org/10.4028/www.scientific.net/amm.423-426.467.

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Cadmium sulfide and cadmium selenide have been the subject of considerable interest because of their potentialapplications in many fields. In this paper, the synthesis of cadmium sulfide and cadmium selenide nanostructures is described. The Morphologies of as prepared cadmium sulfide and cadmium selenide nanostructures are summarized. And the applications and prospects of cadmium sulfide and cadmium selenide in this field also are analyzed.
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Pfaff, Gerhard. "Cadmium sulfide / selenide pigments." Physical Sciences Reviews 6, no. 6 (February 16, 2021): 211–16. http://dx.doi.org/10.1515/psr-2020-0151.

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Abstract Cadmium sulfide and selenide pigments (cadmium pigments) belong to the inorganic yellow, orange and red pigments. Cadmium sulfide pigments are based on the wurtzite lattice, where cadmium can be partially substituted by zinc or mercury and sulfide by selenide. Cadmium pigments are characterized by excellent optical and application characteristics in particular regarding brightness of shade, hiding power, tinting strength, and weather fastness. The declining use of cadmium-containing materials in the last decades is a result of the environmental discussion and the development of less problematic substitute products, especially of bismuth vanadate and high-value organic, temperature-stable yellow and red pigments.
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Антипов, В. В., С. А. Кукушкин, А. В. Осипов, and В. П. Рубец. "Эпитаксиальный рост пленок селенида кадмия на кремнии с буферным слоем карбида кремния." Физика твердого тела 60, no. 3 (2018): 499. http://dx.doi.org/10.21883/ftt.2018.03.45552.275.

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AbstractAn epitaxial cubic 350-nm-thick cadmium selenide has been grown on silicon for the first time by the method of evaporation and condensation in a quasi-closed volume. It is revealed that, in this method, the optimum substrate temperature is 590°C, the evaporator temperature is 660°C, and the growth time is 2 s. To avoid silicon etching by selenium with formation of amorphous SiSe_2, a high-quality ~100-nm-thick buffer silicon carbide layer has been synthesized on the silicon surface by substituting atoms. The powder diffraction pattern and the Raman spectrum unambiguously correspond to cubic cadmium selenide crystal. The ellipsometric, Raman, and electron diffraction analyses demonstrate high structural perfection of the cadmium selenide layer and the absence of a polycrystalline phase.
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Zhang, Ya Hui, Xi Cheng, and Qing Wang. "The Synthesis and Properties of Cadmium Selenide Nanostructures." Advanced Materials Research 531 (June 2012): 63–66. http://dx.doi.org/10.4028/www.scientific.net/amr.531.63.

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Cadmium selenide has been the subject of considerable interest because of its potential applications in many fields. In this paper, the synthesis of cadmium selenide nanostructures is described. The Morphologies of as prepared cadmium selenide nanostructures are summarized. And the applications and prospects of Cadmium selenide in this field also are analyzed.
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Pozdin, Andrey V., Daria D. Smirnova, Larisa N. Maskaeva, Gennady L. Rusinov, and Vyacheslav F. Markov. "Chemical bath synthesis of metal chalcogenide films. Part 41. Hydrochemical deposition of thin films of cadmium selenide by sodium selenosulfate." Butlerov Communications 59, no. 9 (September 30, 2019): 29–39. http://dx.doi.org/10.37952/roi-jbc-01/19-59-9-29.

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The group II-VI semiconductor materials including Cadmium Selenide (CdSe) thin films are widely used in many fields of science and technology, in particular in optoelectronics, nanoelectronics and solar energy. Chemical bath deposition (CBD) represents the simplest and the most available technique for deposition of semiconducting layers. CBD is characterized by deletion of toxic gaseous precursors, operation at low temperature and using of inexpensive equipment. The ionic equilibriums in reaction mixture «CdCl2 – L − Na2SeSO3» (L− NH4OH or Na3C6H5¬O7 or mixture of NH4OH and Na3C6H5¬O7 ) were calculated in present work. The prevailing cadmium complex compounds were determined in appropriate for CBD of cadmium selenide films pH range. The main complex compounds inhibiting fast formation of cadmium selenide are Cd(OH)Cit^(2-) complex (in citrat- and ammonia-citrat mixtures) and 〖Cd(NH_3)〗_5^(2+) complex (in ammonia mixture). Also the boundary conditions of forming CdSe and Cd(OH)2 in reaction mixture were determined by thermodynamic calculation based on crystallization factor to estimate the formation conditions of main (CdSe) and impurity (Cd(OH)2) phases. The results of the calculations show that the solid phase of cadmium selenide is possible to form in pH range from 10 to 14. CdSe films were grown by chemical bath deposition on glass substrates at a temperature of 353 K. The thickness of films ranges from 100 to 220 nm. The grain size of films is about 30 nm which was determined by electron microscopic investigations. The elemental composition of cadmium selenide was defined by energy dispersive analysis; the ratio of cadmium and selenium is 1.03 : 1.16. The conductivity of n-type was determined by the sign of thermoelectromotive force.
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Kowalik, Remigiusz, Honorata Kazimierczak, and Piotr Żabiński. "Electrodeposition of cadmium selenide." Materials Science in Semiconductor Processing 50 (August 2016): 43–48. http://dx.doi.org/10.1016/j.mssp.2016.04.009.

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Ospina, Rogelio, Sergio A. Rincón-Ortiz, and Jhonatan Rodriguez-Pereira. "Cadmium selenide by XPS." Surface Science Spectra 27, no. 1 (June 2020): 014021. http://dx.doi.org/10.1116/6.0000162.

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Türe, I. E., M. Claybourn, A. W. Brinkman, and J. Woods. "Defects in cadmium selenide." Journal of Crystal Growth 72, no. 1-2 (July 1985): 189–93. http://dx.doi.org/10.1016/0022-0248(85)90142-3.

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Zhang, Ya Hui, Xi Cheng, and Qing Wang. "The New Progress on Synthesis of Cadmium Selenide and Lead Selenide Nanostructures." Applied Mechanics and Materials 723 (January 2015): 536–39. http://dx.doi.org/10.4028/www.scientific.net/amm.723.536.

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Cadmium Selenide and Lead Selenide have been the subject of considerable interest because of its potential applications in many fields. In this paper, the synthesis of Cadmium Selenide and Lead Selenide nanostructures is described. The Morphologies of as prepared metal selenide nanostructures are summarized. And the applications and prospects of metal selenide in this field also are analyzed.
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Gao, Yukun, and PG Yin. "Synthesis of cubic CdSe nanocrystals and their spectral properties." Nanomaterials and Nanotechnology 7 (January 1, 2017): 184798041770174. http://dx.doi.org/10.1177/1847980417701747.

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The cadmium selenide nanocrystals are prepared by colloidal chemistry under mild conditions. X-ray diffraction and high-resolution transmission electron microscopy measurements indicate that as-prepared cadmium selenide nanocrystals are zinc blende cubic structure. We carry out an analysis of quantum size effect in the Raman spectra of cadmium selenide nanocrystals performed by utilizing the chemical bond theory of Raman peak shift developed recently. It is revealed that the shifts of Raman peaks in cadmium selenide nanocrystals result from the overlapping of the quantum effect shifts and surface effect shifts. The sizes of the as-prepared cadmium selenide nanocrystals obtained by employing the Raman peak shift theory are in good agreement with the nanocrystal sizes determined by high-resolution transmission electron microscopy.
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Dissertations / Theses on the topic "Cadmium selenide"

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Nguyen, Nu Hoai Vi School of Chemical Engineering &amp Industrial Chemistry UNSW. "Photocatalytic reduction of cadmium and selenium ions and the deposition of cadmium selenide." Awarded by:University of New South Wales. School of Chemical Engineering and Industrial Chemistry, 2005. http://handle.unsw.edu.au/1959.4/20849.

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Titanium dioxide (TiO2) photocatalysis, which can oxidise or reduce organic and inorganic pollutants, is a developing technology for water and wastewater treatment. The current work investigates the photocatalytic reduction of cadmium and selenium species as the presence of these elements in water are of environmental concern. Although TiO2 has been widely used for the photocatalytic process, its light absorption is limited to the UV region of the solar spectrum. Hence, the current project also explores the possibility to deposit cadmium selenide (CdSe) onto TiO2 to extend the photoresponse to the visible region. This study demonstrated that cadmium (Cd(II)) could be reduced to its metallic form by photocatalysis. The choice of hole scavengers and reaction pH are of importance in determining whether the photocatalytic reduction reaction will occur. It is also essential that both Cd(II) and organic additives are adsorbed on the surface of TiO2. A mechanism for cadmium photoreduction in the presence of formate as the hole scavenger was proposed. The current investigation elucidated the mechanism for the photoreduction of selenite (Se(IV)). Selenite was found to be photoreduced to its elemental form (Se(0)) as films, by direct photoreduction of Se(IV), and as discrete particles, by the reaction between Se(IV) and selenide (Se(2-)) ions. The Se(2-) ions are believed to have been generated from the 6 electron photoreduction of Se(IV) and/or the further photoreduction of the Se(0) deposits. Photocatalytic reduction reactions of Se(IV) and selenate (Se(VI)) using different commercial TiO2 materials was also studied. The current work also successfully deposited CdSe by photocatalysis using Se-TiO2 obtained from the photoreduction of Se(IV) and Se(VI). The mechanism for CdSe deposition was clarified and attributed to the reaction of Cd(II) present in the system and the Se(2-) released from the reduction of Se(0) upon further illumination. The Se??TiO2 photocatalysts obtained from the photoreduction of different selenium precursors (Se(IV) and Se(VI)) resulted in the dominance of different morphologies of the CdSe particles. This suggests a new approach to manipulate the properties of CdSe during its formation, and hence control over electrical and optical properties of this semiconductor.
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Roy, Santanu. "Spectroscopic study of defects in cadmium selenide quantum dots (QDS) and cadmium selenide nanorods (NRS)." Diss., Kansas State University, 2013. http://hdl.handle.net/2097/16118.

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Doctor of Philosophy
Department of Chemistry
Viktor Chikan
Ever depleting sources of fossil fuel has triggered more research in the field of alternate sources of energy. Over the past few years, CdSe nanoparticles have emerged as a material with a great potential for optoelectronic applications because of its easy exciton generation and charge separation. Electronic properties of CdSe nanoparticles are highly dependent on their size, shape and electronic environment. The main focus of this research is to explore the effect of different electronic environments on various spectroscopic properties of CdSe nanoparticles and link this to solar cell performance. To attain that goal, CdSe quantum dots (QDs) and nanorods (NRs) have been synthesized and either doped with metal dopants or embedded in polymer matrices. Electronic properties of these nanocomposites have been studied using several spectroscopic techniques such as absorption, photoluminescence, time-resolved photoluminescence, confocal microscopy and wide field microscopy. Indium and tin are the two metal dopants that have been used in the past to study the effect of doping on conductivity of CdSe QDs. Based on the photoluminescence quenching experiments, photoluminescence of both indium and tin doped samples suggest that they behave as n-type semiconductors. A comparison between theoretical and experimental data suggests that energy levels of indium doped and tin doped QDs are 280 meV and 100 meV lower than that of the lowest level of conduction band respectively. CdSe nanorods embedded in two different polymer matrices have been investigated using wide field fluorescence microscopy and confocal microscopy. The data reveals significant enhancement in bandedge luminescence of NRs in the vicinity of a conjugated polymer such as P3HT. Photoactive charge transfer from polymers to the surface traps of NRs may account for the observed behavior. Further study shows anti-correlation between bandedge and trap state emission of CdSe NRs. A recombination model has been proposed to explain the results. The origin of traps is also investigated and plausible explanations are drawn from the acquired data.
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Varanasi, Mohan R. "Geometries of small cadmium selenide (CdSe) clusters." Virtual Press, 2006. http://liblink.bsu.edu/uhtbin/catkey/1349770.

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The sizes, shapes, relaxed atomic positions, eigenvalues, and total energies are calculated for selected ultra-small CdSe clusters using SIESTA, a software package for electronic structure calculations and molecular dynamics simulations of molecules and solids. The properties of these bare clusters with small numbers of constituent atoms are studied using density functional theory (DFT) for energy calculations and the conjugate gradient approximation as well as simulated annealing type of molecular dynamics techniques in relaxing the structure to find the lowest energy configurations.The ab-initio norm-conserving pseudopotentials, the exchange-correlation approximation, and parameters used in the computations by Siesta software is verified using FHI98PP, a package used to generate and test the ab-initio norm-conserving pseudopotentials. The initial position of the atomic co-ordinates is determined using ancillary software written in Matlab.
Department of Physics and Astronomy
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Sacra, Ann. "Stark spectroscopy of cadmium Selenide (CdSe) nanocrystallites." Thesis, Massachusetts Institute of Technology, 1996. http://hdl.handle.net/1721.1/9892.

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Leatherdale, Catherine A. (Catherine Anne) 1972. "Photophysics of cadmium selenide quantum dot solids." Thesis, Massachusetts Institute of Technology, 2000. http://hdl.handle.net/1721.1/8828.

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Thesis (Ph.D.)--Massachusetts Institute of Technology, Dept. of Chemistry, 2000.
Includes bibliographical references.
Semiconductor quantum dots or nanocrystals have size dependent optical and electronic properties that arise from quantum confinement. While the quantum size effect is reasonably well understood, the effect of abrupt interface between the nanocrystal and its dielectric environment is not. In this thesis we study how the dielectric environment affects the quantum dot electronic structure, the optical absorption ~ross-section, charge separation, and transport in cadmium selenide colloidal quantum dots. The electronic states and optical absorption cross-section are found to be less sensitive to changes in the dielectric environment than predicted from theory unless screening from the ligand shell is taken into account. The absolute absorption cross section is measured as a function of quantum dot size; excellent agreement with theory is obtained for absorption far above the band edge. Three-dimensional close packed solids of quantum dots are predicted to act as model artificial solids. Optical absorption measurements indicate that the electronic states of CdSe quantum dots separated by 11 angstroms or more are essentially uncoupled. Photoconductivity measurements suggest that photoexcited quantum confined excitons are ionized by the applied field with a rate that depends on both the size and surface passivation of the quantum dots. The charge generation efficiency decreases with increasing temperature as non-radiative and radiative recombination pathways increasingly compete with charge separation. A simple tunneling model for the initial charge separation step is presented that qualitatively reproduces both the size and surface dependence of the photoconductivity as a function of applied electric field. Finally, we report observations of amplified spontaneous emission from quantum dot solids. The stimulated emission is tunable with quantum dot size and does not sensitively depend upon surface passivation. These measurements demonstrate the feasibility of nanocrystal quantum dot lasers and amplifiers.
by Catherine A. Leatherdale.
Ph.D.
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Nirmal, Manoj. "Photophysics of cadmium selenide (CdSe) semiconductor nanocrystals." Thesis, Massachusetts Institute of Technology, 1996. http://hdl.handle.net/1721.1/10715.

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Stewart, Helen. "Studies into the growth and doping of zinc selenide and zinc cadmium selenide." Thesis, Heriot-Watt University, 1996. http://hdl.handle.net/10399/734.

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Philipp, Dean. "Structural and optical properties of small cadmium selenide nanocyrstallites." Thesis, Massachusetts Institute of Technology, 1995. http://hdl.handle.net/1721.1/38098.

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Sih, Bryan Christian. "Gold and cadmium selenide (CdSe) nanoparticles capped with oligothiophenes." Thesis, University of British Columbia, 2007. http://hdl.handle.net/2429/31523.

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The preparation and characterization of hybrid materials composed of oligothiophene-capped Au and CdSe nanoparticles with novel chemical, structural, electronic and optical properties are reported. α-Phosphino-oligothiophenes (12-15 and 23) and thiol-substituted oligothiophenes (26, 29, 32) were prepared by metal-catalyzed coupling reactions and studied using absorption and emission spectroscopy, and cyclic voltammetry. These functionalized oligothiophenes were used to passivate the surface of Au (16-19) and CdSe (CdSe-26, CdSe-29, CdSe-32) nanoparticles. Oligothiophene-capped Au nanoparticles were prepared directly by reducing a Au salt in the presence of the phosphino-oligothiophene. Attachment to the Au nanoparticles has little effect on the electronic structure of the oligothiophene as determined from the absorption spectra. On the other hand, the oligothiophenes appear to affect the electronic structure of the Au nanoparticle, as observed via a red-shift in the surface plasmon absorption. Electrochemical oxidation of the phosphino-terthiophene capped Au nanoparticles lead to crosslinking where the nanoparticles are linked both structurally and electronically by observed increases in conjugation, conductivity and plasmon coupling relative to the unlinked particles. The oligothiophene bridge linking the Au nanoparticles is shown to facilitate plasmon coupling between adjacent nanoparticles. The crosslinked material also demonstrates tunable conductivity where the conductivity in the material can be increased by oxidative doping of the π-conjugated bridge. Oligothiophene-capped CdSe nanoparticles were prepared through an exchange reaction between thiol-substituted oligothiophenes and trioctylphosphine oxide-capped CdSe nanoparticles. Attachment of the oligothiophenes to the CdSe nanoparticle has little effect on the electronic structure of the oligothiophene as determined from the absorption spectra. However, the optical properties are significantly affected where the oligothiophene emission is quenched after attachment to the CdSe surface due to either an energy or electron transfer mechanism. Depending on the number of oligothiophenes attached to the CdSe surface, the optical properties of the CdSe nanoparticles are affected differently. An excess number of thiols act as hole traps leading to quenching of the nanoparticle emission. Attempts to electrochemically crosslink these oligothiophene-capped CdSe nanoparticles were unsuccessful possibly due to the intrinsic resistivity in the particles.[See Thesis for Diagrams]
Science, Faculty of
Chemistry, Department of
Graduate
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Oduor, A. O. "Electronic transport properties in evaporated cadmium selenide thin films." Thesis, Keele University, 1997. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.388869.

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Books on the topic "Cadmium selenide"

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Rosenberger, F. Growth of zinc selenide single crystals by physical vapor transport in microgravity: Final report, NASA grant NAG8-767, period of performance, 4/1/89 - 8/31/95. Huntsville, Ala: Center for Microgravity and Materials Research, University of Alabama in Huntsville, 1995.

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Rosenberger, F. Growth of zinc selenide single crystals by physical vapor transport in microgravity: Semi-annual progress report, NASA grant NAG8-767, period of performance, 4/1/93 through 10/1/93. Huntsville, Ala: Center for Microgravity and Materials Research, University of Alabama in Huntsville, 1993.

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Patterson, James D. Electronic characterization of defects in narrow gap semiconductors: Comparison of electronic energy levels and formation energies in Mercury Cadmium Telluride Mercury Zinc Telluride and Mercury Zinc Selenide, semi-annual report, September 19, 1994 to March 19, 1995. [Washington, D.C: National Aeronautics and Space Administration, 1995.

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Sillanpää, Mikko. Status of cadmium, lead, cobalt, and selenium in soils and plants of thirty countries. Rome: FAO, 1992.

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Rosenberger, F. Research support for cadmium telluride crystal growth: Sixth semi-annual report, NASA grant NAG8-842, period of performance, 2-11-92 - 8-10-93. Huntsville, Ala: Center for Microgravity and Materials Research, University of Alabama in Huntsviile, 1993.

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Rosenberger, F. Research support for cadmium telluride crystal growth: Final report, NASA grant NAG8-842, period of performance, 8/10/90 - 8/9/95. Huntsville, Ala: Center for Microgravity and Materials Research, University of Alabama in Huntsville, 1995.

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Mason, Robert P. An investigation of the influence of water quality on the mercury, methylmercury, arsenic, selenium, and cadmium concentrations in fish of representative Maryland stream: Final report. Annapolis, MD (580 Taylor Ave., Annapolis 21401): Maryland Dept. of Natural Resources, Chesapeake Bay Research and Monitoring Division, 2002.

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Patterson, James D. Electronic characterization of defects in narrow gap semiconductors: Final report, November 25, 1992 to November 25, 1994. Marshall Space Flight Center, AL: [National Aeronautics and Space Administration], George C. Marshall Space Flight Center, 1994.

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Griepink, B. The certification of the contents (mass fraction) of carbon, hydrogen, nitrogen, chlorine, arsenic, cadmium, manganese, mercury, lead, selenium, vanadium and zinc in three coals: Gas coal CRM No.180, coking coal CRM No.181, steam coal CRM No.182. Luxembourg: Commission of the European Communities, 1986.

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Rodway, Neil Graham. Metal-enhancement of semiconductor emission in a cadmium selenide-gold nanocomposite. 2006.

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Book chapters on the topic "Cadmium selenide"

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Gooch, Jan W. "Cadmium Selenide." In Encyclopedic Dictionary of Polymers, 108. New York, NY: Springer New York, 2011. http://dx.doi.org/10.1007/978-1-4419-6247-8_1802.

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Adachi, Sadao. "Cubic Cadmium Selenide (c-CdSe)." In Optical Constants of Crystalline and Amorphous Semiconductors, 510–16. Boston, MA: Springer US, 1999. http://dx.doi.org/10.1007/978-1-4615-5247-5_39.

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Adachi, Sadao. "Wurtzite Cadmium Selenide (w-CdSe)." In Optical Constants of Crystalline and Amorphous Semiconductors, 517–29. Boston, MA: Springer US, 1999. http://dx.doi.org/10.1007/978-1-4615-5247-5_40.

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Feenstra, R. M., and S. W. Hla. "2.3.5 CdSe, Cadmium Selenide, and CdS, Cadmium Sulfide." In Physics of Solid Surfaces, 49. Berlin, Heidelberg: Springer Berlin Heidelberg, 2015. http://dx.doi.org/10.1007/978-3-662-47736-6_22.

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Sleight, Arthur W., and Harry L. Pinch. "Cadmium Chromium(III) Selenide, CdCr2 Se4." In Inorganic Syntheses, 155–57. Hoboken, NJ, USA: John Wiley & Sons, Inc., 2007. http://dx.doi.org/10.1002/9780470132456.ch33.

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Adachi, Sadao. "Cadmium Sulpho-Selenide (CdS x Se1-x )." In Optical Constants of Crystalline and Amorphous Semiconductors, 579–81. Boston, MA: Springer US, 1999. http://dx.doi.org/10.1007/978-1-4615-5247-5_49.

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Adachi, Sadao. "Zinc Cadmium Selenide (Zn x Cd1-x Se)." In Optical Constants of Crystalline and Amorphous Semiconductors, 563–66. Boston, MA: Springer US, 1999. http://dx.doi.org/10.1007/978-1-4615-5247-5_45.

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Adachi, Sadao. "Mercury Cadmium Selenide (Hg1-x Cd x Se)." In Optical Constants of Crystalline and Amorphous Semiconductors, 585–87. Boston, MA: Springer US, 1999. http://dx.doi.org/10.1007/978-1-4615-5247-5_51.

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Yang, Jun, and Hui Liu. "Cadmium Selenide–Platinum Nanocomposites with a Core–Shell Construction." In Metal-Based Composite Nanomaterials, 115–41. Cham: Springer International Publishing, 2014. http://dx.doi.org/10.1007/978-3-319-12220-5_5.

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Kumar, Suresh, and K. P. Tiwary. "Cadmium Selenide Thin Film Deposition and Characterization for Photovoltaic Applications." In Materials Horizons: From Nature to Nanomaterials, 333–67. Singapore: Springer Nature Singapore, 2022. http://dx.doi.org/10.1007/978-981-19-0553-7_9.

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Conference papers on the topic "Cadmium selenide"

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PRUDNIKAU, A., and M. ARTEMYEV. "OPTICAL PROPERTIES OF CADMIUM SELENIDE NANOCRYSTALS WITH CADMIUM SUBSTITUTION BY MERCURY." In Proceedings of International Conference Nanomeeting – 2011. WORLD SCIENTIFIC, 2011. http://dx.doi.org/10.1142/9789814343909_0043.

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TSELIKOV, G., V. TIMOSHENKO, and S. DOROFEEV. "PHOTOLUMINESCENCE PROPERTIES OF CADMIUM SELENIDE QUANTUM DOTS." In Proceedings of International Conference Nanomeeting – 2011. WORLD SCIENTIFIC, 2011. http://dx.doi.org/10.1142/9789814343909_0045.

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Gosnell, Jonathan D., Michael A. Schreuder, Michael J. Bowers II, Sandra J. Rosenthal, and Sharon M. Weiss. "Cadmium selenide nanocrystals as white-light phosphors." In SPIE Optics + Photonics, edited by Ian T. Ferguson, Nadarajah Narendran, Tsunemasa Taguchi, and Ian E. Ashdown. SPIE, 2006. http://dx.doi.org/10.1117/12.680774.

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Rath, M. C., A. Guleria, S. Singh, A. K. Singh, S. Adhikari, and S. K. Sarkar. "Electron beam assisted synthesis of cadmium selenide nanomaterials." In SOLID STATE PHYSICS: PROCEEDINGS OF THE 57TH DAE SOLID STATE PHYSICS SYMPOSIUM 2012. AIP, 2013. http://dx.doi.org/10.1063/1.4791097.

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Dey, Mrinmoy, Mahmudul Hasan, Rahat Amin, and Maitry Dey. "Numerical analysis of efficient cadmium selenide solar cell." In 2017 3rd International Conference on Electrical Information and Communication Technology (EICT). IEEE, 2017. http://dx.doi.org/10.1109/eict.2017.8275247.

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Bentley, Sean J., Charles V. Anderson, and John P. Dooher. "Three-photon absorption in cadmium selenide quantum dots." In 2006 Conference on Lasers and Electro-Optics and 2006 Quantum Electronics and Laser Science Conference. IEEE, 2006. http://dx.doi.org/10.1109/cleo.2006.4628335.

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Cheung, William, Salvador Montes, Erik Sousa, Liangmin Zhang, Ivan O. Mondragon, Anthony Linares-Garcia, David Bishel, Joseph Mini, and Lifeng Dong. "Deposition of cadmium sulfide and cadmium selenide thin films using chemical bath deposition technique." In Quantum Dots and Nanostructures: Growth, Characterization, and Modeling XV, edited by Diana L. Huffaker and Holger Eisele. SPIE, 2018. http://dx.doi.org/10.1117/12.2309748.

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Murali, K. R., V. Subramanian, N. Rangarajan, A. S. Lakshmanan, and S. K. Rangarajan. "Photoconducting and photoelectrochemical characteristics of selectively plated cadmium selenide films." In San Dieg - DL Tentative, edited by Richard I. Seddon. SPIE, 1990. http://dx.doi.org/10.1117/12.22393.

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More, Anup J., Sachin A. Pawar, Vishal V. Burungale, Raghunath S. Patil, and Pramod S. Patil. "Hybrid polymer solar cell based on cadmium selenide quantum dots." In PROCEEDING OF INTERNATIONAL CONFERENCE ON RECENT TRENDS IN APPLIED PHYSICS AND MATERIAL SCIENCE: RAM 2013. AIP, 2013. http://dx.doi.org/10.1063/1.4810176.

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Shah, Nidhi, S. M. Vyas, Piyush Patel, Vimal Patel, Himanshu Pavagadhi, and M. P. Jani. "Study of dielectric characteristics of bulk cadmium selenide (CdSe) pellet." In 3RD INTERNATIONAL CONFERENCE ON CONDENSED MATTER AND APPLIED PHYSICS (ICC-2019). AIP Publishing, 2020. http://dx.doi.org/10.1063/5.0001221.

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Reports on the topic "Cadmium selenide"

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Doyle, Kevin, and Sudhir Trivedi. Dislocation Etching Solutions for Mercury Cadmium Selenide. Fort Belvoir, VA: Defense Technical Information Center, September 2014. http://dx.doi.org/10.21236/ada609573.

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Roy, U. N., G. S. Camarda, Y. Cui, R. Gul, A. Hossain, and G. Yang. Cadmium Zinc Telluride Selenide (CdZnTeSe) A promising low cost alternative to Cadmium Zinc Telluride (CdZnTe) for medical imaging and nuclear detector applications. Office of Scientific and Technical Information (OSTI), June 2017. http://dx.doi.org/10.2172/1376113.

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Veblen, D. R., and E. S. Ilton. HRTEM/AEM and SEM study of fluid-rock interactions: Interaction of copper, silver, selenium, chromium, and cadmium-bearing solutions with geological materials at near surface conditions, with an emphasis on phyllosilicates. Office of Scientific and Technical Information (OSTI), May 1992. http://dx.doi.org/10.2172/7075474.

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